Dimethyl Sulfoxide (DMSO) Decreases Cell Proliferation and TNF-α, IFN-γ, and IL-2 Cytokines Production in Cultures of Peripheral Blood Lymphocytes

Dimethylsulfoxide (DMSO) is an amphipathic molecule composed of a polar domain characterized by the sulfinyl and two nonpolar methyl groups, for this reason it is able to solubilize polar and nonpolar substances and transpose hydrophobic barriers. DMSO is widely used to solubilize drugs of therapeut...

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Published inMolecules (Basel, Switzerland) Vol. 22; no. 11; p. 1789
Main Authors De Abreu Costa, Lucas, Henrique Fernandes Ottoni, Marcelo, Dos Santos, Michaelle, Meireles, Agnes, Gomes de Almeida, Valéria, De Fátima Pereira, Wagner, Alves de Avelar-Freitas, Bethânia, Eustáquio Alvim Brito-Melo, Gustavo
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 10.11.2017
MDPI
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ISSN1420-3049
1420-3049
DOI10.3390/molecules22111789

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Abstract Dimethylsulfoxide (DMSO) is an amphipathic molecule composed of a polar domain characterized by the sulfinyl and two nonpolar methyl groups, for this reason it is able to solubilize polar and nonpolar substances and transpose hydrophobic barriers. DMSO is widely used to solubilize drugs of therapeutic applications and studies indicated that 10% v/v concentration did not modify culture viability when used to treat human peripheral blood mononuclear cells (PBMC). However, some DMSO concentrations could influence lymphocyte activation and present anti-inflammatory effects. Therefore, the objective of this study was to evaluate the effect of DMSO on lymphocyte activation parameters. Cell viability analysis, proliferation, and cytokine production were performed on PBMC from six healthy subjects by flow cytometry. The results indicated that 2.5% v/v DMSO concentrations did not modify lymphocytes viability. DMSO at 1% and 2% v/v concentrations reduced the relative proliferation index of lymphocytes and at 5% and 10% v/v concentrations reduced the percentage of total lymphocytes, cluster of differentiation 4+ (CD4+) T lymphocytes and CD8+ T lymphocytes interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α) and interleukin-2 (IL-2) producers. Thus, it was concluded that DMSO has an in vitro anti-inflammatory effect by reducing lymphocyte activation demonstrated with proliferation reduction and the decrease of cytokine production.
AbstractList Dimethylsulfoxide (DMSO) is an amphipathic molecule composed of a polar domain characterized by the sulfinyl and two nonpolar methyl groups, for this reason it is able to solubilize polar and nonpolar substances and transpose hydrophobic barriers. DMSO is widely used to solubilize drugs of therapeutic applications and studies indicated that 10% v/v concentration did not modify culture viability when used to treat human peripheral blood mononuclear cells (PBMC). However, some DMSO concentrations could influence lymphocyte activation and present anti-inflammatory effects. Therefore, the objective of this study was to evaluate the effect of DMSO on lymphocyte activation parameters. Cell viability analysis, proliferation, and cytokine production were performed on PBMC from six healthy subjects by flow cytometry. The results indicated that 2.5% v/v DMSO concentrations did not modify lymphocytes viability. DMSO at 1% and 2% v/v concentrations reduced the relative proliferation index of lymphocytes and at 5% and 10% v/v concentrations reduced the percentage of total lymphocytes, cluster of differentiation 4+ (CD4+) T lymphocytes and CD8+ T lymphocytes interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α) and interleukin-2 (IL-2) producers. Thus, it was concluded that DMSO has an in vitro anti-inflammatory effect by reducing lymphocyte activation demonstrated with proliferation reduction and the decrease of cytokine production.
Dimethylsulfoxide (DMSO) is an amphipathic molecule composed of a polar domain characterized by the sulfinyl and two nonpolar methyl groups, for this reason it is able to solubilize polar and nonpolar substances and transpose hydrophobic barriers. DMSO is widely used to solubilize drugs of therapeutic applications and studies indicated that 10% concentration did not modify culture viability when used to treat human peripheral blood mononuclear cells (PBMC). However, some DMSO concentrations could influence lymphocyte activation and present anti-inflammatory effects. Therefore, the objective of this study was to evaluate the effect of DMSO on lymphocyte activation parameters. Cell viability analysis, proliferation, and cytokine production were performed on PBMC from six healthy subjects by flow cytometry. The results indicated that 2.5% DMSO concentrations did not modify lymphocytes viability. DMSO at 1% and 2% concentrations reduced the relative proliferation index of lymphocytes and at 5% and 10% concentrations reduced the percentage of total lymphocytes, cluster of differentiation 4⁺ (CD4⁺) T lymphocytes and CD8⁺ T lymphocytes interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α) and interleukin-2 (IL-2) producers. Thus, it was concluded that DMSO has an in vitro anti-inflammatory effect by reducing lymphocyte activation demonstrated with proliferation reduction and the decrease of cytokine production.
Dimethylsulfoxide (DMSO) is an amphipathic molecule composed of a polar domain characterized by the sulfinyl and two nonpolar methyl groups, for this reason it is able to solubilize polar and nonpolar substances and transpose hydrophobic barriers. DMSO is widely used to solubilize drugs of therapeutic applications and studies indicated that 10% v/v concentration did not modify culture viability when used to treat human peripheral blood mononuclear cells (PBMC). However, some DMSO concentrations could influence lymphocyte activation and present anti-inflammatory effects. Therefore, the objective of this study was to evaluate the effect of DMSO on lymphocyte activation parameters. Cell viability analysis, proliferation, and cytokine production were performed on PBMC from six healthy subjects by flow cytometry. The results indicated that 2.5% v/v DMSO concentrations did not modify lymphocytes viability. DMSO at 1% and 2% v/v concentrations reduced the relative proliferation index of lymphocytes and at 5% and 10% v/v concentrations reduced the percentage of total lymphocytes, cluster of differentiation 4⁺ (CD4⁺) T lymphocytes and CD8⁺ T lymphocytes interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α) and interleukin-2 (IL-2) producers. Thus, it was concluded that DMSO has an in vitro anti-inflammatory effect by reducing lymphocyte activation demonstrated with proliferation reduction and the decrease of cytokine production.Dimethylsulfoxide (DMSO) is an amphipathic molecule composed of a polar domain characterized by the sulfinyl and two nonpolar methyl groups, for this reason it is able to solubilize polar and nonpolar substances and transpose hydrophobic barriers. DMSO is widely used to solubilize drugs of therapeutic applications and studies indicated that 10% v/v concentration did not modify culture viability when used to treat human peripheral blood mononuclear cells (PBMC). However, some DMSO concentrations could influence lymphocyte activation and present anti-inflammatory effects. Therefore, the objective of this study was to evaluate the effect of DMSO on lymphocyte activation parameters. Cell viability analysis, proliferation, and cytokine production were performed on PBMC from six healthy subjects by flow cytometry. The results indicated that 2.5% v/v DMSO concentrations did not modify lymphocytes viability. DMSO at 1% and 2% v/v concentrations reduced the relative proliferation index of lymphocytes and at 5% and 10% v/v concentrations reduced the percentage of total lymphocytes, cluster of differentiation 4⁺ (CD4⁺) T lymphocytes and CD8⁺ T lymphocytes interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α) and interleukin-2 (IL-2) producers. Thus, it was concluded that DMSO has an in vitro anti-inflammatory effect by reducing lymphocyte activation demonstrated with proliferation reduction and the decrease of cytokine production.
Author Dos Santos, Michaelle
De Abreu Costa, Lucas
Henrique Fernandes Ottoni, Marcelo
Meireles, Agnes
Alves de Avelar-Freitas, Bethânia
Gomes de Almeida, Valéria
De Fátima Pereira, Wagner
Eustáquio Alvim Brito-Melo, Gustavo
AuthorAffiliation 3 Institute of Science and Technology, Federal University of the Jequitinhonha and Mucuri Valleys, Diamantina, MG 39100-000, Brazil
1 Immunology Laboratory, Integrated Center for Health Research, Federal University of the Jequitinhonha and Mucuri Valleys (UFVJM), Diamantina, MG 39100-000, Brazil; lucas.farmac@gmail.com (L.d.A.C.); m.ottoni@yahoo.com.br (M.H.F.O.); michaellegsantos@gmail.com (M.G.d.S.); agnesbm@gmail.com (A.B.M.); valeria.g.almeida@gmail.com (V.G.d.A.); wagnerufvjm@gmail.com (W.d.F.P.); gbrito1998@yahoo.com (G.E.A.B.-M.)
2 Multicenter Graduate Program in Physiological Sciences/UFVJM Graduate Program in Pharmaceutical Sciences/UFVJM, Federal University of the Jequitinhonha and Mucuri Valleys, Diamantina, MG 39100-000, Brazil
4 Graduate Program in Dentistry, School of Dentistry, Federal University of the Jequitinhonha and Mucuri Valleys, Diamantina, MG 39100-000, Brazil
AuthorAffiliation_xml – name: 3 Institute of Science and Technology, Federal University of the Jequitinhonha and Mucuri Valleys, Diamantina, MG 39100-000, Brazil
– name: 2 Multicenter Graduate Program in Physiological Sciences/UFVJM Graduate Program in Pharmaceutical Sciences/UFVJM, Federal University of the Jequitinhonha and Mucuri Valleys, Diamantina, MG 39100-000, Brazil
– name: 1 Immunology Laboratory, Integrated Center for Health Research, Federal University of the Jequitinhonha and Mucuri Valleys (UFVJM), Diamantina, MG 39100-000, Brazil; lucas.farmac@gmail.com (L.d.A.C.); m.ottoni@yahoo.com.br (M.H.F.O.); michaellegsantos@gmail.com (M.G.d.S.); agnesbm@gmail.com (A.B.M.); valeria.g.almeida@gmail.com (V.G.d.A.); wagnerufvjm@gmail.com (W.d.F.P.); gbrito1998@yahoo.com (G.E.A.B.-M.)
– name: 4 Graduate Program in Dentistry, School of Dentistry, Federal University of the Jequitinhonha and Mucuri Valleys, Diamantina, MG 39100-000, Brazil
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  givenname: Lucas
  surname: De Abreu Costa
  fullname: De Abreu Costa, Lucas
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  givenname: Marcelo
  orcidid: 0000-0002-2333-2775
  surname: Henrique Fernandes Ottoni
  fullname: Henrique Fernandes Ottoni, Marcelo
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  givenname: Michaelle
  surname: Dos Santos
  fullname: Dos Santos, Michaelle
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  givenname: Agnes
  surname: Meireles
  fullname: Meireles, Agnes
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  givenname: Valéria
  surname: Gomes de Almeida
  fullname: Gomes de Almeida, Valéria
– sequence: 6
  givenname: Wagner
  surname: De Fátima Pereira
  fullname: De Fátima Pereira, Wagner
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  givenname: Bethânia
  surname: Alves de Avelar-Freitas
  fullname: Alves de Avelar-Freitas, Bethânia
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  givenname: Gustavo
  orcidid: 0000-0001-6138-7235
  surname: Eustáquio Alvim Brito-Melo
  fullname: Eustáquio Alvim Brito-Melo, Gustavo
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29125561$$D View this record in MEDLINE/PubMed
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Issue 11
Keywords anti-inflammatory agents
solvents
dimethyl sulfoxide
Language English
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Snippet Dimethylsulfoxide (DMSO) is an amphipathic molecule composed of a polar domain characterized by the sulfinyl and two nonpolar methyl groups, for this reason it...
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SubjectTerms anti-inflammatory agents
Cell Death - drug effects
Cell Proliferation - drug effects
Cells, Cultured
Cytokines
dimethyl sulfoxide
Dimethyl Sulfoxide - pharmacology
Hemolysis - drug effects
Humans
Interferon-gamma - biosynthesis
Interleukin-2 - biosynthesis
Lymphocyte receptors
Lymphocytes
Lymphocytes - cytology
Lymphocytes - drug effects
Lymphocytes - metabolism
solvents
T cell receptors
Tumor Necrosis Factor-alpha - biosynthesis
Tumor necrosis factor-TNF
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Title Dimethyl Sulfoxide (DMSO) Decreases Cell Proliferation and TNF-α, IFN-γ, and IL-2 Cytokines Production in Cultures of Peripheral Blood Lymphocytes
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